T!Write Report Writing - Data & Statistical Analysis
The key to the success of clinical trials is the design of your trial. The design very much depends on the actual purpose of the trial. T!Write can support the (clinical) study design development for client's initiating clinical trials or other research.
Clinical development
The key to the success of clinical trials is the design of your trial. Read More
Data management
T!Write is experienced in the management and analysis... Read More
Medical Writing
T!Write offers medical writing in English and Dutch. Read More
Services
The key to the success of clinical trials is the design of your trial. The design very much depends on the actual purpose of the trial. T!Write can support the (clinical) study design development for client's initiating clinical trials or other research.
Advise in (clinical) study design
Advise in setting the objectives and related endpoints and performance goals
Sample size determination
Advise in Case Report Form (CRF) development and data collection
T!Write is experienced in the management and analysis of reserach data in general and in advanced statistical methods for interim & final analysis and stopping rules. T!Write’s statistical data analysis department provides an unbiased interpretation of the results of pharmaceutical or mechanical interventions.
The statistical data analysts are trained to perform adequate assessments and are blinded to the randomization sequence whenever possible or needed. The statistical data analysis department reduces inter-observer variability and increases the accuracy and precision of results, establishing and overseeing compliance to protocol, guidelines and the statistical analysis plan (SAP).
T!Write offers medical writing in English and Dutch. Results of data analysis are reported according relevant guidelines. The following documents can be prepared and provided:
Statistical sections in Clinical Protocols
Statistical Analysis Plan (SAP) including tables, listings and graphs (TLG)